NCT Number: NCT02615288
High Dose Vitamin D3 in Crohn's Disease
This is a randomized, double-blind placebo-controlled trial of high dose vitamin D3 at 10,000 International Units (IU) daily compared to low dose at 1000 IU daily in patients with Crohn's disease in remission.
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Notify MeKey information
Conditions
Age range
18 year–70 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
About this study
In patients with Crohn's disease in remission, the investigators hypothesized higher doses of vitamin D would more effectively improve 25-hydroxy(OH)-vitamin D levels and would be tolerated well without side effects of hypercalcemia. The investigators also wanted to explore whether higher doses could reduce the clinical relapse rate of patients with Crohn's disease in remission, and if higher doses of vitamin D3 could improve depression and anxiety symptoms. In order to determine if there is benefit from high-dose vitamin D3, the investigators designed a pilot randomized double-blind controlled trial comparing doses of oral vitamin D3 at 10,000 IU daily to 1000 IU daily.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- a prior diagnosis of Crohn's disease in clinical remission for at least 28 days with a Harvey-Bradshaw index less than or equal to 4
- All maintenance therapies for Crohn's disease will be required to be at stable dose for at least 3 months before randomization, with no systemic steroid therapy within 4 weeks.
- Vitamin D supplements will be discontinued at least 6 weeks before randomization.
Exclusion criteria
- Women of child bearing potential who are considering pregnancy during the study period, currently pregnant, or unwilling to use contraception to avoid pregnancy
- Participants with renal insufficiency (serum creatinine greater than 150 umol/L), sarcoidosis, hyperparathyroidism, malignancy, or any other disorder that may lead to hypercalcemia
- Patients with short-gut syndrome or a serum albumin less than 32 g/L
- Concomitant therapy with thiazide diuretics, barbiturates, digitalis, or supplemental products containing vitamin D
Treatment and study plan
Primary outcomes
-
Improvement in 25-OH vitamin D level
Time frame: One year
Secondary outcomes
-
Clinical Remission (defined as Harvey-Bradshaw index <=4)
Time frame: One year
Number of patients who maintain clinical remission
-
Improvement in Depression scores (measured by Hospital Anxiety and Depression Scale (HADS))
Time frame: One year
Number of patients who achieve significant improvement in HADS (reduction of 2 or more)
-
Improvement in C-reactive protein
Time frame: One year
Comparison of C-reactive protein levels in high and low dose vitamin D3 groups
-
Adverse events
Time frame: One year
Number of patients with treatment-related adverse events, including death, hypercalcemia, and hospitalization, as well as minor adverse events
Sponsors and collaborators
Lead sponsor
McMaster University
Other
Collaborators
- Canadian Association of Gastroenterology
Registry information
Official study title
Impact of High Dose Vitamin D3 Supplementation in Treatment of Crohn's Disease in Remission: A Randomized Double-blind Controlled Study
Important dates
- Study start
- 2014
- Primary completion
- 2015
- First posted
- Nov 26, 2015
- Registry last updated
- Nov 26, 2015
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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